Canonical Allele Identifier: CA423821650

Gene: RYR2

Linked Data

• gnomAD v4: 1-237678097-C-A
• MyVariant Identifiers: chr1:g.237841397C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.237678097C>A , CM000663.2:g.237678097C>A	GRCh38
NC_000001.10:g.237841397C>A , CM000663.1:g.237841397C>A	GRCh37
NC_000001.9:g.235908020C>A	NCBI36
NG_008799.2:g.640696C>A
NG_008799.3:g.640914C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609119.2:c.8831-2359C>A	ENSP00000499659.2:n.8831-2359C>A
ENST00000659194.3:c.8880C>A	ENSP00000499653.3:p.Ile2960=
ENST00000660292.2:c.8880C>A	ENSP00000499787.2:p.Ile2960=
ENST00000659194.2:c.1069C>A
ENST00000366574.7:c.8880C>A MANE Select	ENSP00000355533.2:p.Ile2960=
ENST00000659194.1:c.1069C>A
ENST00000360064.7:c.8832C>A	ENSP00000353174.7:p.Ile2944=
ENST00000366574.6:c.8880C>A	ENSP00000355533.2:p.Ile2960=
ENST00000609119.1:n.84-2359C>A
NM_001035.2:c.8880C>A	NP_001026.2:p.Ile2960=
XM_006711802.2:c.8910C>A	XP_006711865.1:p.Ile2970=
XM_006711803.2:c.8907C>A	XP_006711866.1:p.Ile2969=
XM_006711804.2:c.8910C>A	XP_006711867.1:p.Ile2970=
XM_006711805.2:c.8880C>A	XP_006711868.1:p.Ile2960=
XM_006711806.2:c.8910C>A	XP_006711869.1:p.Ile2970=
XM_006711807.2:c.8910C>A	XP_006711870.1:p.Ile2970=
XM_006711808.2:c.8860+3251C>A	XP_006711871.1:n.8860+3251C>A
XM_006711810.2:c.8877C>A	XP_006711873.1:p.Ile2959=
XR_949152.1:n.9191C>A
XM_006711802.3:c.8910C>A	XP_006711865.1:p.Ile2970=
XM_006711803.3:c.8907C>A	XP_006711866.1:p.Ile2969=
XM_006711804.3:c.8910C>A	XP_006711867.1:p.Ile2970=
XM_006711805.3:c.8880C>A	XP_006711868.1:p.Ile2960=
XM_006711806.3:c.8910C>A	XP_006711869.1:p.Ile2970=
XM_006711807.3:c.8910C>A	XP_006711870.1:p.Ile2970=
XM_006711808.3:c.8860+3251C>A	XP_006711871.1:n.8860+3251C>A
XM_006711810.3:c.8877C>A	XP_006711873.1:p.Ile2959=
XM_017002028.1:c.8889C>A	XP_016857517.1:p.Ile2963=
XR_949152.2:n.9224C>A
NM_001035.3:c.8880C>A MANE Select	NP_001026.2:p.Ile2960=